Kaixian X. Du
Zhengzhou, 450052, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications
Clinical and genetic characteristics of X-linked intellectual disability associated with HUWE1 gene variants
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: November 13, 2025
Identification of CDK5RAP2 as a causative gene of focal epilepsy without microcephaly.
Journal: Seizure
Published: June 09, 2025
Haploinsufficiency of brain-specific kinase BRSK1 causes epilepsy and neurodevelopmental disorders.
Journal: Epilepsia
Published: February 15, 2025
Clinical and genetic spectrum of 6 cases with asparagine synthetase deficiency
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: March 25, 2024
Corrigendum: Different frequency bands in various regions of the brain play different roles in the onset and wake-sleep stages of infantile spasms.
Journal: Frontiers in pediatrics
Published: January 11, 2023
Clinical and genetic analysis of two patients with CHARGE syndrome due to de novo variants of CHD7 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 21, 2022
Different Frequency Bands in Various Regions of the Brain Play Different Roles in the Onset and Wake-Sleep Stages of Infantile Spasms.
Journal: Frontiers in pediatrics
Published: February 17, 2022
An intractable epilepsy phenotype of ASNS novel mutation in two patients with asparagine synthetase deficiency.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: January 27, 2022
Clinical and genetic spectrum of SCN2A gene associated epilepsy and episodic ataxia
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: January 06, 2022
Last Updated: 09/26/2026